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Clinical Trials Europe

Ensure Trial Success Through Building Effective Partnerships and Implementing Strong Outsourcing Strategies

Collaborate and Achieve Goals with Expert Guidance from Leading Stakeholder Perspectives

Providing a thorough overview of partnership and outsourcing strategy, regulatory updates, RWE and data privacy

Explore the Essential Updates with Panel Discussions, Live Q&As, Case Studies and more

Latest Learnings with Real World Evidence:

  • Hear a joint presentation on Real World Data in Practice- Perspectives from the MHRA and a Clinician 
  • Examples of Real World Data and evidence and how it was implemented
  • AstraZeneca will discuss how they developed a quality management checklist to support audits of Real-World Data (RWD) used in regulatory submissions.
  • Participate in an interactive discussion addressing: Real World Evidence – Experiences

Partnership, Outsourcing, Regulatory Updates and Data Privacy:

  • Hear a Case Study from GSK’s on FSP Partnership, Critical Factors for FSP Transition of Sponsor Studies
  • Join the debate - What does long term partnerships really mean?
  • Regulatory best practices of the clinical trial regulation and the accelerated clinical trials in EU, HMA, EMA and EU commission initiative
  • Learnings on the impact and industry perspective for EU Clinical Trial Regulation 536/2014 from Seagen